ClinGen Allele Registry
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Canonical Allele Identifier:
CA337441774
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrY:g.19768401T>C
GRCh37
chrY:g.21930287T>C
Linked Data - Sequence & Population
gnomAD v3:
Y:19768401 T / C
gnomAD v4:
chrY-19768401-T-C
Joint Max Group AF
0.01443598 (EAS)
Genomes Max Group AF
0.01443598 (EAS)
Linked Data - NCBI & NCI
dbSNP:
2032614
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000024.10:g.19768401T>C , CM000686.2:g.19768401T>C
GRCh38
NC_000024.9:g.21930287T>C , CM000686.1:g.21930287T>C
GRCh37
NC_000024.8:g.20389675T>C
NCBI36
Search 100 bp 5'
Search 100 bp 3'